Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
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Alliance of Genome Resources | October 9, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
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DOID:0060230 | basal ganglia calcification | MGI:97851 | Mus musculus (house mouse) | 20516 | Slc20a2 |
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DOID:0080042 | autosomal recessive spinocerebellar ataxia 18 | MGI:95813 | Mus musculus (house mouse) | 14804 | Grid2 |
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DOID:0050635 | alternating hemiplegia of childhood | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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DOID:10487 | Hirschsprung's disease | MGI:102720 | Mus musculus (house mouse) | 13618 | Ednrb |
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DOID:3911 | progeria | MGI:96794 | Mus musculus (house mouse) | 16905 | Lmna |
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DOID:0050548 | hereditary sensory neuropathy | MGI:97383 | Mus musculus (house mouse) | 18211 | Ntrk1 |
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DOID:0111960 | immunodeficiency 15A | MGI:1338071 | Mus musculus (house mouse) | 16150 | Ikbkb |
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DOID:0111731 | familial episodic pain syndrome 3 | MGI:1345149 | Mus musculus (house mouse) | 24046 | Scn11a |
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DOID:14720 | Ehlers-Danlos syndrome classic type 1 | MGI:88457 | Mus musculus (house mouse) | 12831 | Col5a1 |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | MGI:2676312 | Mus musculus (house mouse) | 74591 | Abca12 |
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DOID:9452 | steatotic liver disease | MGI:96765 | Mus musculus (house mouse) | 16835 | Ldlr |
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DOID:0050540 | Charcot-Marie-Tooth disease type 3 | MGI:103177 | Mus musculus (house mouse) | 17528 | Mpz |
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DOID:2749 | glycogen storage disease Ia | MGI:95607 | Mus musculus (house mouse) | 14377 | G6pc1 |
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DOID:0070538 | syndromic X-linked intellectual developmental disorder bain type | MGI:1201779 | Mus musculus (house mouse) | 56258 | Hnrnph2 |
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DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | MGI:87868 | Mus musculus (house mouse) | 11409 | Acads |
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DOID:0110943 | autosomal recessive osteopetrosis 2 | MGI:1100089 | Mus musculus (house mouse) | 21943 | Tnfsf11 |
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DOID:0110495 | autosomal recessive nonsyndromic deafness 37 | MGI:104785 | Mus musculus (house mouse) | 17920 | Myo6 |
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DOID:0080047 | pseudoachondroplasia | MGI:88469 | Mus musculus (house mouse) | 12845 | Comp |
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DOID:9352 | type 2 diabetes mellitus | MGI:87853 | Mus musculus (house mouse) | 50518 | a |
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DOID:0050558 | Ullrich congenital muscular dystrophy | MGI:88459 | Mus musculus (house mouse) | 12833 | Col6a1 |
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DOID:1206 | Rett syndrome | MGI:99918 | Mus musculus (house mouse) | 17257 | Mecp2 |
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DOID:1909 | melanoma | MGI:88190 | Mus musculus (house mouse) | 109880 | Braf |
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DOID:0060649 | congenital hereditary endothelial dystrophy of cornea | MGI:2138987 | Mus musculus (house mouse) | 269356 | Slc4a11 |
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DOID:0080462 | developmental and epileptic encephalopathy 7 | MGI:1309503 | Mus musculus (house mouse) | 16536 | Kcnq2 |
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DOID:0090144 | Donnai-Barrow syndrome | MGI:95794 | Mus musculus (house mouse) | 14725 | Lrp2 |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024